Canonical Allele Identifier: CA714361014
Gene: ADAM10 HGNC NCBI

Linked Data

dbSNP Id: rs139857169
MyVariant Identifiers: chr15:g.59042081G>C (hg19) chr15:g.58749882G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749882G>C , CM000677.2:g.58749882G>C GRCh38
NC_000015.9:g.59042081G>C , CM000677.1:g.59042081G>C GRCh37
NC_000015.8:g.56829373G>C NCBI36
NG_033876.1:g.5097C>G
NG_033876.2:g.4826C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-348C>G ENSP00000260408.3:n.-348C>G
NM_001110.3:c.-348C>G NP_001101.1:n.-348C>G
NM_001320570.1:c.-348C>G NP_001307499.1:n.-348C>G
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